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Health Effects of Chronic Arsenic Exposure

  • Hong, Young-Seoub (Heavy Metal Exposure Environmental Health Center, Dong-A University) ;
  • Song, Ki-Hoon (Department of Dermatology, Dong-A University College of Medicine) ;
  • Chung, Jin-Yong (Heavy Metal Exposure Environmental Health Center, Dong-A University)
  • Received : 2014.08.17
  • Accepted : 2014.09.03
  • Published : 2014.09.30

Abstract

Arsenic is a unique element with distinct physical characteristics and toxicity whose importance in public health is well recognized. The toxicity of arsenic varies across its different forms. While the carcinogenicity of arsenic has been confirmed, the mechanisms behind the diseases occurring after acute or chronic exposure to arsenic are not well understood. Inorganic arsenic has been confirmed as a human carcinogen that can induce skin, lung, and bladder cancer. There are also reports of its significant association to liver, prostate, and bladder cancer. Recent studies have also suggested a relationship with diabetes, neurological effects, cardiac disorders, and reproductive organs, but further studies are required to confirm these associations. The majority of research to date has examined cancer incidence after a high exposure to high concentrations of arsenic. However, numerous studies have reported various health effects caused by chronic exposure to low concentrations of arsenic. An assessment of the health effects to arsenic exposure has never been performed in the South Korean population; thus, objective estimates of exposure levels are needed. Data should be collected on the biological exposure level for the total arsenic concentration, and individual arsenic concentration by species. In South Korea, we believe that biological exposure assessment should be the first step, followed by regular health effect assessments.

Keywords

References

  1. Agency for Toxic Substances and Disease Registry. Toxicological profile for arsenic; 2007 [cited 2014 Sep 16]. Available from: http://www.atsdr.cdc.gov/toxprofiles/tp2.pdf.
  2. Tchounwou PB, Wilson B, Ishaque A. Important considerations in the development of public health advisories for arsenic and arsenic-containing compounds in drinking water. Rev Environ Health 1999;14(4):211-229.
  3. Rousselot P, Labaume S, Marolleau JP, Larghero J, Noguera MH, Brouet JC, et al. Arsenic trioxide and melarsoprol induce apoptosis in plasma cell lines and in plasma cells from myeloma patients. Cancer Res 1999;59(5):1041-1048.
  4. Mandal BK, Ogra Y, Suzuki KT. Identification of dimethylarsinous and monomethylarsonous acids in human urine of the arsenic-affected areas in West Bengal, India. Chem Res Toxicol 2001;14(4):371-378. https://doi.org/10.1021/tx000246h
  5. International Agency For Research On Cancer. IARC monographs on the evaluation of carcinogen risks to humans; 2004 [cited 2014 Sep 16]. Available from: http://monographs.iarc.fr/ENG/Monographs/vol83/mono83.pdf.
  6. Environmental Protection Agency. An exposure and risk assessment for arsenic; 1982 [cited 2014 Sep 16]. Available from: http://nepis.epa.gov/Exe/ZyPURL.cgi?Dockey=2000M05S.TXT.
  7. Marchiset-Ferlay N, Savanovitch C, Sauvant-Rochat MP. What is the best biomarker to assess arsenic exposure via drinking water? Environ Int 2012;39(1):150-171. https://doi.org/10.1016/j.envint.2011.07.015
  8. Cho Y, Seo S, Choi SH, Lee S, Kim K, Kim HJ, et al. Association of arsenic levels in soil and water with urinary arsenic concentration of residents in the vicinity of closed metal mines. Int J Hyg Environ Health 2013;216(3):255-262. https://doi.org/10.1016/j.ijheh.2012.05.003
  9. Hanlon DP, Ferm VH. Placental permeability of arsenate ion during early embryogenesis in the hamster. Experientia 1977;33(9):1221-1222. https://doi.org/10.1007/BF01922340
  10. Tchounwou PB, Patlolla AK, Centeno JA. Carcinogenic and systemic health effects associated with arsenic exposure: a critical review. Toxicol Pathol 2003;31(6):575-588.
  11. Buchet JP, Lauwerys R, Roels H. Urinary excretion of inorganic arsenic and its metabolites after repeated ingestion of sodium metaarsenite by volunteers. Int Arch Occup Environ Health 1981;48(2):111-118. https://doi.org/10.1007/BF00378431
  12. Centeno JA, Gray MA, Mullick FG, Tchounwou PB, Tseng C. Arsenic in drinking water and health issues. In: Moore TA, Black A, Centeno JA, Harding JS, Trumm DA. Metal contaminants in New Zealand: sources, treatments, and effects on ecology and hu man health. Christchurch: Resolutionz Press; 2005, p. 195-219.
  13. Abernathy CO, Liu YP, Longfellow D, Aposhian HV, Beck B, Fowler B, et al. Arsenic: health effects, mechanisms of actions, and research issues. Environ Health Perspect 1999;107(7):593-597. https://doi.org/10.1289/ehp.99107593
  14. Goyer RA. Toxic effects of metals. In: Casarett LJ, Doull J, Klaassen CD. Casarett and Doull's toxicology: the basic science of poisons. 6th ed. New York: McGraw-Hill; 2001, p. 811-867.
  15. Hughes MF. Arsenic toxicity and potential mechanisms of action. Toxicol Lett 2002;133(1):1-16. https://doi.org/10.1016/S0378-4274(02)00084-X
  16. Centeno JA, Tchounwou PB, Patlolla AK, Mullick FG, Murakata L, Meza E, et al. Environmental pathology and health effects of arsenic poisoning: a critical review. In: Naidu R, Smith E, Owens G, Bhattacharya P, Nadebaum P. Managing arsenic in the environment: from soil to human health. Collingwood: CSIRO Publishing; 2006, p. 311-327.
  17. Arsenic and arsenic compounds. IARC Monogr Eval Carcinog Risk Chem Hum 1980;23:39-141.
  18. Kapaj S, Peterson H, Liber K, Bhattacharya P. Human health effects from chronic arsenic poisoning: a review. J Environ Sci Health A Tox Hazard Subst Environ Eng 2006;41(10):2399-2428. https://doi.org/10.1080/10934520600873571
  19. Chen CJ, Kuo TL, Wu MM. Arsenic and cancers. Lancet 1988;1(8582):414-415.
  20. Kurokawa M, Ogata K, Idemori M, Tsumori S, Miyaguni H, Inoue S, et al. Investigation of skin manifestations of arsenicism due to intake of arsenic-contaminated groundwater in residents of Samta, Jessore, Bangladesh. Arch Dermatol 2001;137(1):102-103.
  21. Smith AH, Goycolea M, Haque R, Biggs ML. Marked increase in bladder and lung cancer mortality in a region of Northern Chile due to arsenic in drinking water. Am J Epidemiol 1998;147(7):660-669. https://doi.org/10.1093/oxfordjournals.aje.a009507
  22. Hopenhayn-Rich C, Biggs ML, Smith AH. Lung and kidney cancer mortality associated with arsenic in drinking water in Cordoba, Argentina. Int J Epidemiol 1998;27(4):561-569. https://doi.org/10.1093/ije/27.4.561
  23. Rossman TG, Uddin AN, Burns FJ. Evidence that arsenite acts as a cocarcinogen in skin cancer. Toxicol Appl Pharmacol 2004;198(3):394-404. https://doi.org/10.1016/j.taap.2003.10.016
  24. Hsueh YM, Chiou HY, Huang YL, Wu WL, Huang CC, Yang MH, et al. Serum beta-carotene level, arsenic methylation capability, and incidence of skin cancer. Cancer Epidemiol Biomarkers Prev 1997;6(8):589-596.
  25. Luster MI, Simeonova PP. Arsenic and urinary bladder cell proliferation. Toxicol Appl Pharmacol 2004;198(3):419-423. https://doi.org/10.1016/j.taap.2003.07.017
  26. Leonardi G, Vahter M, Clemens F, Goessler W, Gurzau E, Hemminki K, et al. Inorganic arsenic and basal cell carcinoma in areas of Hungary, Romania, and Slovakia: a case-control study. Environ Health Perspect 2012;120(5):721-726. https://doi.org/10.1289/ehp.1103534
  27. Ferreccio C, Gonzalez C, Milosavjlevic V, Marshall G, Sancha AM, Smith AH. Lung cancer and arsenic concentrations in drinking water in Chile. Epidemiology 2000;11(6):673-679. https://doi.org/10.1097/00001648-200011000-00010
  28. Smith AH, Marshall G, Yuan Y, Ferreccio C, Liaw J, von Ehrenstein O, et al. Increased mortality from lung cancer and bronchiectasis in young adults after exposure to arsenic in utero and in early childhood. Environ Health Perspect 2006;114(8)1293-1296. https://doi.org/10.1289/ehp.8832
  29. Chiou HY, Hsueh YM, Liaw KF, Horng SF, Chiang MH, Pu YS, et al. Incidence of internal cancers and ingested inorganic arsenic: a seven-year follow-up study in Taiwan. Cancer Res 1995;55(6):1296-1300.
  30. Chiu HF, Ho SC, Yang CY. Lung cancer mortality reduction after installation of tap-water supply system in an arseniasis-endemic area in Southwestern Taiwan. Lung Cancer 2004;46(3)265-270.
  31. Chen CL, Hsu LI, Chiou HY, Hsueh YM, Chen SY, Wu MM, et al. Ingested arsenic, cigarette smoking, and lung cancer risk: a follow-up study in arseniasis-endemic areas in Taiwan. JAMA 2004;292(24):2984-2990. https://doi.org/10.1001/jama.292.24.2984
  32. Garcia-Esquinas E, Pollan M, Umans JG, Francesconi KA, Goessler W, Guallar E, et al. Arsenic exposure and cancer mortality in a US-based prospective cohort: the strong heart study. Cancer Epidemiol Biomarkers Prev 2013;22(11):1944-1953. https://doi.org/10.1158/1055-9965.EPI-13-0234-T
  33. Chiang HS, Guo HR, Hong CL, Lin SM, Lee EF. The incidence of bladder cancer in the black foot disease endemic area in Taiwan. Br J Urol 1993;71(3):274-278. https://doi.org/10.1111/j.1464-410X.1993.tb15942.x
  34. Gabriel HE, Crott JW, Ghandour H, Dallal GE, Choi SW, Keyes MK, et al. Chronic cigarette smoking is associated with diminished folate status, altered folate form distribution, and increased genetic damage in the buccal mucosa of healthy adults. Am J Clin Nutr 2006;83(4):835-841.
  35. Gamble MV, Liu X, Slavkovich V, Pilsner JR, Ilievski V, Factor-Litvak P, et al. Folic acid supplementation lowers blood arsenic. Am J Clin Nutr 2007;86(4):1202-1209.
  36. Meliker JR, Slotnick MJ, AvRuskin GA, Schottenfeld D, Jacquez GM, Wilson ML, et al. Lifetime exposure to arsenic in drinking water and bladder cancer: a population-based case-control study in Michigan, USA. Cancer Causes Control 2010;21(5)745-757.
  37. Morales KH, Ryan L, Kuo TL, Wu MM, Chen CJ. Risk of internal cancers from arsenic in drinking water. Environ Health Perspect 2000;108(7):655-661. https://doi.org/10.1289/ehp.00108655
  38. Baastrup R, Sorensen M, Balstrom T, Frederiksen K, Larsen CL, Tjonneland A, et al. Arsenic in drinking-water and risk for cancer in Denmark. Environ Health Perspect 2008;116(2):231-237.
  39. Lin HJ, Sung TI, Chen CY, Guo HR. Arsenic levels in drinking water and mortality of liver cancer in Taiwan. J Hazard Mater 2013;262:1132-1138. https://doi.org/10.1016/j.jhazmat.2012.12.049
  40. Durant JL, Chen J, Hemond HF, Thilly WG. Elevated incidence of childhood leukemia in Woburn, Massachusetts: NIEHS Superfund Basic Research Program searches for causes. Environ Health Perspect 1995;103 Suppl 6:93-98. https://doi.org/10.1289/ehp.95103s693
  41. Heck JE, Park AS, Qiu J, Cockburn M, Ritz B. Risk of leukemia in relation to exposure to ambient air toxics in pregnancy and early childhood. Int J Hyg Environ Health 2014;217(6):662-668. https://doi.org/10.1016/j.ijheh.2013.12.003
  42. Tsai SY, Chou HY, The HW, Chen CM, Chen CJ. The effects of chronic arsenic exposure from drinking water on the neurobehavioral development in adolescence. Neurotoxicology 2003;24(4-5):747-753. https://doi.org/10.1016/S0161-813X(03)00029-9
  43. Wasserman GA, Liu X, Parvez F, Ahsan H, Factor-Litvak P, van Geen A, et al. Water arsenic exposure and children's intellectual function in Araihazar, Bangladesh. Environ Health Perspect 2004;112(13):1329-1333. https://doi.org/10.1289/ehp.6964
  44. Lai MS, Hsueh YM, Chen CJ, Shyu MP, Chen SY, Kuo TL, et al. Ingested inorganic arsenic and prevalence of diabetes mellitus. Am J Epidemiol 1994;139(5):484-492. https://doi.org/10.1093/oxfordjournals.aje.a117031
  45. Tseng CH, Tseng CP, Chiou HY, Hsueh YM, Chong CK, Chen CJ. Epidemiologic evidence of diabetogenic effect of arsenic. Toxicol Lett 2002;133(1):69-76. https://doi.org/10.1016/S0378-4274(02)00085-1
  46. Nizam S, Kato M, Yatsuya H, Khalequzzaman M, Ohnuma S, Naito H, et al. Differences in urinary arsenic metabolites between diabetic and non-diabetic subjects in Bangladesh. Int J Environ Res Public Health 2013;10(3):1006-1019. https://doi.org/10.3390/ijerph10031006
  47. Ahsan H, Perrin M, Rahman A, Parvez F, Stute M, Zheng Y, et al. Associations between drinking water and urinary arsenic levels and skin lesions in Bangladesh. J Occup Environ Med 2000;42(12):1195-1201. https://doi.org/10.1097/00043764-200012000-00016
  48. Ahsan H, Chen Y, Parvez F, Zablotska L, Argos M, Hussain I, et al. Arsenic exposure from drinking water and risk of premalignant skin lesions in Bangladesh: baseline results from the Health Effects of Arsenic Longitudinal Study. Am J Epidemiol 2006;163(12):1138-1148. https://doi.org/10.1093/aje/kwj154
  49. Lee MY, Bae ON, Chung SM, Kang KT, Lee JY, Chung JH. Enhancement of platelet aggregation and thrombus formation by arsenic in drinking water: a contributing factor to cardiovascular disease. Toxicol Appl Pharmacol 2002;179(2):83-88. https://doi.org/10.1006/taap.2001.9356
  50. Chakraborti D, Mukherjee SC, Pati S, Sengupta MK, Rahman MM, Chowdhury UK, et al. Arsenic groundwater contamination in Middle Ganga Plain, Bihar, India: a future danger? Environ Health Perspect 2003;111(9):1194-1201. https://doi.org/10.1289/ehp.5966
  51. Hopenhayn C, Huang B, Christian J, Peralta C, Ferreccio C, Atallah R, et al. Profile of urinary arsenic metabolites during pregnancy. Environ Health Perspect 2003;111(16):1888-1891. https://doi.org/10.1289/ehp.6254
  52. Chattopadhyay S, Bhaumik S, Purkayastha M, Basu S, Nag Chaudhuri A, Das Gupta S. Apoptosis and necrosis in developing brain cells due to arsenic toxicity and protection with antioxidants. Toxicol Lett 2002;136(1):65-76. https://doi.org/10.1016/S0378-4274(02)00282-5
  53. Hopenhayn C, Ferreccio C, Browning SR, Huang B, Peralta C, Gibb H, et al. Arsenic exposure from drinking water and birth weight. Epidemiology 2003;14(5):593-602. https://doi.org/10.1097/01.ede.0000072104.65240.69
  54. Kile ML, Hoffman E, Hsueh YM, Afroz S, Quamruzzaman Q, Rahman M, et al. Variability in biomarkers of arsenic exposure and metabolism in adults over time. Environ Health Perspect 2009;117(3):455-460. https://doi.org/10.1289/ehp.11251
  55. Loffredo CA, Aposhian HV, Cebrian ME, Yamauchi H, Silbergeld EK. Variability in human metabolism of arsenic. Environ Res 2003;92(2):85-91. https://doi.org/10.1016/S0013-9351(02)00081-6
  56. Bae HS, Ryu DY, Choi BS, Park JD. Urinary arsenic concentrations and their associated factors in Korean adults. Toxicol Res 2013;29(2):137-142. https://doi.org/10.5487/TR.2013.29.2.137
  57. Eom SY, Lee YC, Yim DH, Lee CH, Kim YD, Choi BS, et al. Effects of low-level arsenic exposure on urinary N-acetyl-$\beta$-D-glucosa- minidase activity. Hum Exp Toxicol 2011;30(12):1885-1891. https://doi.org/10.1177/0960327111402239
  58. Chowdhury UK, Rahman MM, Sengupta MK, Lodh D, Chanda CR, Roy S, et al. Pattern of excretion of arsenic compounds [arsenite, arsenate, MMA(V), DMA(V)] in urine of children compared to adults from an arsenic exposed area in Bangladesh. J Environ Sci Health A Tox Hazard Subst Environ Eng 2003;38(1)87-113. https://doi.org/10.1081/ESE-120016883
  59. Wen W, Wen J, Lu L, Liu H, Yang J, Cheng H, et al. Metabolites of arsenic and increased DNA damage of p53 gene in arsenic plant workers. Toxicol Appl Pharmacol 2011;254(1):41-47. https://doi.org/10.1016/j.taap.2011.04.013
  60. Hsueh YM, Chung CJ, Shiue HS, Chen JB, Chiang SS, Yang MH, et al. Urinary arsenic species and CKD in a Taiwanese population: a case-control study. Am J Kidney Dis 2009;54(5):859-870. https://doi.org/10.1053/j.ajkd.2009.06.016

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  56. Cohort profile: health effects monitoring programme in Ndilo, Dettah and Yellowknife (YKHEMP) vol.10, pp.9, 2020, https://doi.org/10.1136/bmjopen-2020-038507
  57. Arsenic and Selenium Profile in Erythrocytes of Renal Transplant Recipients vol.197, pp.2, 2014, https://doi.org/10.1007/s12011-019-02021-w
  58. Elemental Composition and Associated Health Risk of Honey Obtained from Apiary Farms in Southeast Nigeria vol.83, pp.10, 2020, https://doi.org/10.4315/jfp-20-072
  59. Rapid and Highly Sensitive Extended Gate FET-Based Sensors for Arsenite Detection Using a Handheld Device vol.9, pp.11, 2014, https://doi.org/10.1149/2162-8777/abab18
  60. Distribution of essential and non-essential elements in rice located in a Protected Natural Reserve “Marjal de Pego-Oliva” vol.94, pp.None, 2014, https://doi.org/10.1016/j.jfca.2020.103654
  61. RETRACTED: Identification of practical amendments to mitigate soil arsenic levels in peas vol.16, pp.None, 2014, https://doi.org/10.1016/j.rhisph.2020.100268
  62. A review on fly ash from coal-fired power plants: chemical composition, regulations, and health evidence vol.35, pp.4, 2014, https://doi.org/10.1515/reveh-2019-0039
  63. Application and efficacy of low-cost adsorbents for metal removal from contaminated water: A review vol.43, pp.p5, 2014, https://doi.org/10.1016/j.matpr.2021.01.316
  64. Recent progress on electrochemical sensing strategies as comprehensive point-care method vol.152, pp.1, 2021, https://doi.org/10.1007/s00706-020-02732-0
  65. Blood lead concentration among oral/inhaled opium users: systematic review and meta-analysis vol.51, pp.1, 2014, https://doi.org/10.1080/10408444.2020.1864722
  66. Effects of arsenic and heavy metals on metabolic pathways in cells of human origin: Similarities and differences vol.8, pp.None, 2021, https://doi.org/10.1016/j.toxrep.2021.05.015
  67. Human Health Risk Assessment of Heavy Metals and Metalloids in Herbal Medicines Used to Treat Anxiety: Monitoring of Safety vol.12, pp.None, 2014, https://doi.org/10.3389/fphar.2021.772928
  68. The Response of the Associations of Grass and Epichloë Endophytes to the Increased Content of Heavy Metals in the Soil vol.10, pp.3, 2014, https://doi.org/10.3390/plants10030429
  69. A review on electrochemical treatment of arsenic from aqueous medium vol.208, pp.3, 2014, https://doi.org/10.1080/00986445.2020.1715956
  70. Miniaturized electrochemical biosensor based on whole‐cell for heavy metal ions detection in water vol.118, pp.4, 2021, https://doi.org/10.1002/bit.27646
  71. Arsenic release through refractory gold ore processing. Immobilization and decontamination approaches vol.20, pp.None, 2014, https://doi.org/10.1016/j.coesh.2021.100236
  72. Detection, Distribution and Health Risk Assessment of Toxic Heavy Metals/Metalloids, Arsenic, Cadmium, and Lead in Goat Carcasses Processed for Human Consumption in South-Eastern Nigeria vol.10, pp.4, 2014, https://doi.org/10.3390/foods10040798
  73. Neuroglobin alleviates arsenic-induced neuronal damage vol.84, pp.None, 2014, https://doi.org/10.1016/j.etap.2021.103604
  74. Long non-coding RNA DICER1-AS1-low expression in arsenic-treated A549 cells inhibits cell proliferation by regulating the cell cycle pathway vol.84, pp.None, 2014, https://doi.org/10.1016/j.etap.2021.103617
  75. Increase of glycogen storage by sodium arsenite in rat cortical astrocytes through glycogen synthase activation and its association to toxicity vol.13, pp.2, 2014, https://doi.org/10.1007/s13530-021-00094-6
  76. Elemental composition of teff (a gluten-free grain), maize and wheat: Staple crops in the Main Ethiopian Rift Valley vol.100, pp.None, 2014, https://doi.org/10.1016/j.jfca.2020.103660
  77. Synthesis, characterization and application of magnetic nanoparticles modified with Fe-Mn binary oxide for enhanced removal of As(III) and As(V) vol.42, pp.16, 2021, https://doi.org/10.1080/09593330.2019.1705919
  78. Stormwater Runoff Treatment Using Pervious Concrete Modified with Various Nanomaterials: A Comprehensive Review vol.13, pp.15, 2014, https://doi.org/10.3390/su13158552
  79. GIS, Multivariate Statistics Analysis and Health Risk Assessment of Water Supply Quality for Human Use in Central Mexico vol.13, pp.16, 2014, https://doi.org/10.3390/w13162196
  80. Molecular Mechanism of Arsenic-Induced Neurotoxicity including Neuronal Dysfunctions vol.22, pp.18, 2014, https://doi.org/10.3390/ijms221810077
  81. Polyaniline/Nanomaterial Composites for the Removal of Heavy Metals by Adsorption: A Review vol.5, pp.9, 2014, https://doi.org/10.3390/jcs5090233
  82. Sex-specific neurotoxic effects of heavy metal pollutants: Epidemiological, experimental evidence and candidate mechanisms vol.201, pp.None, 2014, https://doi.org/10.1016/j.envres.2021.111558
  83. Assessment of Trace Elements Supply in Canned Tuna Fish Commercialized for Human Consumption in Brazil vol.18, pp.22, 2014, https://doi.org/10.3390/ijerph182212002
  84. Metals and Metal-Nanoparticles in Human Pathologies: From Exposure to Therapy vol.26, pp.21, 2021, https://doi.org/10.3390/molecules26216639
  85. Defining drinking water metal contaminant mixture risk by coupling zebrafish behavioral analysis with citizen science vol.11, pp.1, 2021, https://doi.org/10.1038/s41598-021-96244-4
  86. Coenzyme Q10 protected against arsenite and enhanced the capacity of 2,3-dimercaptosuccinic acid to ameliorate arsenite-induced toxicity in mice vol.22, pp.1, 2014, https://doi.org/10.1186/s40360-021-00484-z
  87. Mitochondrial Dysfunction in Arsenic-Induced Hepatotoxicity: Pathogenic and Therapeutic Implications vol.200, pp.1, 2014, https://doi.org/10.1007/s12011-021-02624-2
  88. The removal of arsenic from solution through biochar-enhanced precipitation of calcium-arsenic derivatives vol.292, pp.no.pa, 2014, https://doi.org/10.1016/j.envpol.2021.118241
  89. Integrating SNPs-based genetic risk factor with blood epigenomic response of differentially arsenic-exposed rural subjects reveals disease-associated signaling pathways vol.292, pp.no.pa, 2014, https://doi.org/10.1016/j.envpol.2021.118279
  90. Heavy metal toxicity, sources, and remediation techniques for contaminated water and soil vol.25, pp.None, 2014, https://doi.org/10.1016/j.eti.2021.102114